
pmid: 9107111
handle: 11454/35068
It is generally accepted that there are two subsets of septo-optic dysplasia (deMorsier's syndrome), one with schizencephaly and the other without schizencephaly. A third form of the anomaly which is associated with callosal absence has also been described. Except for schizencephaly, the association of septo-optic dysplasia with another major type of disorder of neuronal migration and organization such as cortical dysplasia, has not yet been reported. We report the MR imaging examination of a 3-year-old patient with bilateral rolandic cortical dysplasia, and with apparent thinning of the optic nerves, and absent septum pellucidum (septo-optic dysplasia) as a new combination. This can be labelled as cortico-septo-optic dysplasia.
Optic Nerve, Kallmann Syndrome, Magnetic Resonance Imaging, brain, magnetic resonance, Frontal Lobe, septo-optic dysplasia, Child, Preschool, brain, abnormalities and anomalies, Humans, Female, Septum Pellucidum, Agenesis of Corpus Callosum, congenital malformations
Optic Nerve, Kallmann Syndrome, Magnetic Resonance Imaging, brain, magnetic resonance, Frontal Lobe, septo-optic dysplasia, Child, Preschool, brain, abnormalities and anomalies, Humans, Female, Septum Pellucidum, Agenesis of Corpus Callosum, congenital malformations
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